Atlas FDA

Revive Reusable Bladder Support

FDA 510(k) clearance K183468 · decided 2019-01-25

Clearance details

K-number
K183468
Device name
Revive Reusable Bladder Support
Applicant
Rinovum Subsidiary 2, LLC
Decision
Substantially Equivalent
Date received
2018-12-14
Decision date
2019-01-25
Days to decision
42 days
Clearance type
Traditional
Product code
HHW
Device class
2
Regulation number
884.3575
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Monroeville, PA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Milex™ Incontinence Dish Pessaries; Milex™ Incontinence Dish Pessaries with Support; Milex™ Cube Pessaries; Milex™ Cube Pessaries with Drainage Holes (K253698)Cooper Surgical2026-01-20
CooperSurgical Milex® Pessaries (K250438)CooperSurgical, Inc.2025-04-11
Cntrl+ Bladder Support Pessary (K240798)Cntrl+, Inc.2024-12-17
Reia pessary (K232677)Reia, LLC2024-05-21
Yoni.Fit Bladder Support (K232525)Watkins-Conti Products, Inc.2024-05-17
Uresta® (K233548)Resilia, Inc.2024-04-03
Gynethotics™ Pessary (K231786)Cosm Medical2024-03-06
ProVate Vaginal Support (K190277)Contipi Medical , Ltd.2019-07-08
Panpac Flexi Shelf Pessary (K173351)Panpac Medical Corporation2018-10-31
Panpac Disposable Pessary Fitting Set (K153422)Panpac Medical Corporation2016-07-14
Always/Tampax bladder supports (K151413)Procter & Gamble2015-12-18
PESSARY (K132313)Eis Corporation2014-12-05

Recalls involving this device

No recalls on record reference this clearance.